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Retinal disorders v1.204 | ADGRV1 | Ivone Leong Phenotypes for gene: ADGRV1 were changed from Usher syndrome, type 2C; Eye Disorders to Usher syndrome, type 2C, 605472; Eye Disorders; Usher syndrome, type 2C, GPR98/PDZD7 digenic, 605472 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Retinal disorders v1.159 | ADGRV1 | Gavin Arno reviewed gene: ADGRV1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Retinal disorders v1.137 | ADGRV1 |
Ivone Leong Source NHS GMS was added to ADGRV1. Rating Changed from Green List (high evidence) to Green List (high evidence) |
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Retinal disorders | ADGRV1 | BRIDGE consortium reviewed ADGRV1 |